prairie-willi

The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros
The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros 1080 608 Oriol Capell
The endowment will serve to finance the clinical trial of an innovative therapy for patients with Fragile X Syndrome and the discovery and clinical development of new PDE-10 inhibitors for the treatment of Prader-Willi syndrome read more
Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome
Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome 1080 675 Guillem Cebrian

Prader-Willi syndrome (PWS) is a disease of uncommon genetic origin considered, however, the most common cause of genetic obesity. According to data extracted from the web portal of the Spanish SPW Association, this disease affects one in 15.000 newborns. A scientific article on this disease was recently published in The Journal of Clinical Endocrinology & Metabolism with the participation of several international researchers who are experts in this syndrome. Among them is Dr.…

read more
Privacy preferences

When you visit our website, your browser may store information about specific services, usually in the form of cookies. Here you can change your privacy preferences. Please note that blocking certain types of cookies may affect your experience on our website and the services we offer.

Enable / disable Google Analytics tracking code
Enable / disable Google Fonts
Turn Google Maps on / off
Enable / disable embedded videos
This website uses cookies, mainly from third party services. You can edit your privacy preferences and / or accept the use of cookies.